Lubricating oil composition for timepiece and timepiece

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a National Stage of International Application No. PCT/JP2014/050454, filed Jan. 14, 2014 (claiming priority based on Japanese Patent Application No. 2013-009330, filed Jan. 22, 2013), the contents of which are incorporated herein by reference in their entirety.

TECHNICAL FIELD

The present invention relates to a lubricating oil composition for a timepiece and a timepiece. More particularly, the present invention relates to a lubricating oil composition for a timepiece, which comprises a lubricant component containing a base oil, an antiwear agent and an antioxidant, and a timepiece having a sliding part to which the lubricating oil composition has been applied.

BACKGROUND ART

Timepieces are broadly classified into mechanical timepieces and electronic timepieces. The mechanical timepieces are timepieces that work by using, as a driving source, a mainspring encased in a barrel, and the electronic timepieces are timepieces that work by utilizing electric force. The mechanical and the electronic timepieces both display a time by combining a wheel train part, in which wheels to drive an hour hand, a minute hand and a second hand are assembled, with sliding parts, such as a lever.

In both timepieces, a lubricating oil composition is applied to the sliding parts in order to make smooth movement. As lubricating oil compositions for timepieces, a lubricating oil composition comprising at least 0.1 to 20% by weight of a viscosity index improver and 0.1 to 8% by weight of an antiwear agent in addition to a base oil composed of a polyol ester, a lubricating oil composition comprising at least 0.1 to 15% by weight of a viscosity index improver in addition to a base oil composed of a paraffin-based hydrocarbon oil having 30 or more carbon atoms, and a lubricating oil composition comprising at least an antiwear agent and an antioxidant in addition to a base oil composed of an ether oil, wherein the antiwear agent is a neutral phosphate ester and/or a neutral phosphite ester, and the content of the antiwear agent is 0.1 to 8% by weight are disclosed in Patent Literature 1.

CITATION LIST
Patent Literature

Patent Literature 1: WO 01/59043

SUMMARY OF INVENTION
Technical Problem

However, if such a conventional lubricating oil composition as described above is applied to sliding parts to operate a timepiece, a deposit such as worn powder or rust is formed in a sliding part to which great pressure is applied during sliding, and the color of the sliding part sometimes changes to dark brown. Thus, there is room for improvement in wear resistance and extreme pressure properties of the conventional lubricating oil compositions. Examples of the sliding parts to which great pressure is applied include sliding parts of mechanical timepieces and sliding parts of electronic timepieces designed so as to have, for example, many motors.

Solution to Problem

The lubricating oil composition for a timepiece according to the present invention is a lubricating oil composition comprising a lubricant component (A) containing at least one base oil (A1) selected from a polyol ester (A-1), a paraffin-based hydrocarbon oil (A-2) having 25 or more carbon atoms and an ether oil (A-3), at least one antiwear agent (B) selected from a neutral phosphate ester (B-1) and a neutral phosphite ester (B-2) and an antioxidant (C), and is characterized in that the total acid number of the composition is not more than 0.8 mgKOH/g, the antiwear agent (B) is contained in an amount of 0.1 to 15 parts by mass based on 100 parts by mass of the lubricant component (A), and the antioxidant (C) is contained in an amount of 0.01 to 3 parts by mass based on 100 parts by mass of the lubricant component (A), and the neutral phosphate ester (B-1) is represented by the following general formula (b-1) and the neutral phosphite ester (B-2) is represented by the following general formula (b-2):

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wherein R^b11to R^b14each independently represent an aliphatic hydrocarbon group of 10 to 16 carbon atoms, R^b15to R^b18each independently represent a straight-chain or branched alkyl group of 1 to 6 carbon atoms, R^b191and R^b192each independently represent a hydrogen atom or a straight-chain or branched alkyl group of 1 to 5 carbon atoms, and the total number of carbon atoms of R^b191and R^b192is 1 to 5,

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wherein R^b21to R^b24each independently represent an aliphatic hydrocarbon group of 10 to 16 carbon atoms, R^b25to R^b28each independently represent a straight-chain or branched alkyl group of 1 to 6 carbon atoms, R^b291and R^b292each independently represent a hydrogen atom or a straight-chain or branched alkyl group of 1 to 5 carbon atoms, and the total number of carbon atoms of R^b291and R^b292is 1 to 5.

Advantageous Effects of Invention

Even when the lubricating oil composition for a timepiece of the present invention is used to a sliding part to which great pressure is applied to operate a timepiece, formation of a deposit such as worn powder or rust can be suppressed, and change in color of the sliding part hardly occurs. That is to say, according to the lubricating oil composition for a timepiece of the present invention, even a mechanical timepiece or the like in which high pressure is applied to its sliding part can be favorably lubricated.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a view to show a sliding part after a timepiece operating test is carried out with regard to Example 1-6-1.

FIG. 2 is a view to show a sliding part after a timepiece operating test is carried out with regard to Comparative Example 1-2.

DESCRIPTION OF EMBODIMENTS

The present invention is specifically described hereinafter.

[Lubricating Oil Composition for Timepiece]

When the total acid number is in this range, there is generally no change in consumption current, and a rise of viscosity and corrosion of timepiece members can be prevented, so that such a total acid number is preferable for a lubricating oil composition for a timepiece. If the components contained and their quantities used are within the ranges described below, the total acid number of the lubricating oil composition becomes not more than 0.8 mgKOH/g, preferably not more than 0.2 mgKOH/g. The total acid number is a value measured in accordance with JIS K2501-5.

In the present invention, the “lubricant component” is used to generically refer to the aforesaid base oil and a solid lubricant. In the present invention, as the lubricant component (A), at least a base oil (A1) is used, and a solid lubricant (A2) can be used together with the base oil (A1). That is to say, the “lubricant component” in the present invention is the base oil (A1) itself or a combination of the base oil (A1) and the solid lubricant (A2).

In the present invention, the content of the base oil (A1) is usually not less than 30% by mass, preferably not less than 40% by mass, based on 100% by mass of the lubricant component (A). Here, the total amount of the base oil (A1) and the solid lubricant (A2) is 100% by mass of the lubricant component (A).

As embodiments of the lubricating oil composition, the following first embodiment and second embodiment can be mentioned.

For example, in the first embodiment of the present invention, the content of the base oil (A1) is more than 70% by mass, preferably not less than 80% by mass, more preferably not less than 90% by mass, particularly preferably 100% by mass, based on 100% by mass of the lubricant component (A).

By using the base oil (A1) in the above amount as the lubricant component (A) and by using an antiwear agent (B) and an antioxidant (C) together with such a lubricant component (A), the lubricating oil composition exhibits excellent wear resistance and extreme pressure properties. The lubricating oil composition of this first embodiment can be preferably used particularly for lubrication of sliding parts possessed by a timepiece, such as a wheel train part.

For example, in the second embodiment of the present invention, a solid lubricant (A2) is used as the lubricant component (A) together with the base oil (A1). Based on 100% by mass of the lubricant component (A), the content of the base oil (A1) is 30 to 70% by mass and the content of the solid lubricant (A2) is 70 to 30% by mass, it is preferable that the content of the base oil (A1) is 40 to 60% by mass and the content of the solid lubricant (A2) is 60 to 40% by mass, and it is more preferable that the content of the base oil (A1) is 40 to 52% by mass and the content of the solid lubricant (A2) is 60 to 48% by mass.

By using the base oil (A1) and the solid lubricant (A2) in the above amounts as the lubricant components (A) and by using an antiwear agent (B) and an antioxidant (C) together with such lubricant components (A), the lubricating oil composition has the aforesaid excellent wear resistance and extreme pressure properties and favorably functions as a lubricant particularly for a portion to which high pressure is applied. The lubricating oil composition of this second embodiment can be preferably used particularly for lubrication of sliding parts possessed by a timepiece, such as a mainspring encased in a barrel.

From the viewpoint of low-temperature properties, it is preferable that the lubricating oil composition of the second embodiment does not contain a thickener. The thickener is a component known as a basic component of grease.

The lubricating oil composition of the second embodiment can have, at ordinary temperature, fluidity of the same level as that of conventional grease containing a base oil, a thickener and an additive. However, this lubricating oil composition does not need to contain a thickener differently from the conventional grease. On this account, the lubricating oil composition of the second embodiment is not solidified even in a low-temperature environment (e.g., −30° C.). That is to say, the lubricating oil composition of the second embodiment can be applied to the same uses as those of the conventional grease, and is excellent in low-temperature properties.

custom character Base Oil (A1)

The base oil (A1) for use in the present invention is at least one kind selected from a polyol ester (A-1), a paraffin-based hydrocarbon oil (A-2) having 25 or more carbon atoms and an ether oil (A-3).

Polyol Ester (A-1)

The polyol ester (A-1) is specifically an ester having a structure obtained by allowing a polyol having two or more hydroxyl groups in one molecule to react with one kind or plural kinds of monobasic acids or acid chlorides.

Examples of the polyols include neopentyl glycol, trimethylolpropane, pentaerythritol and dipentaerythritol.

Examples of the monobasic acids include saturated aliphatic carboxylic acids, such as acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, pivalic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, lauric acid, myristic acid and palmitic acid;

unsaturated aliphatic carboxylic acids, such as stearic acid, acrylic acid, propiolic acid, crotonic acid and oleic acid; and

cyclic carboxylic acids, such as benzoic acid, toluic acid, naphthoic acid, cinnamic acid, cyclohexanecarboxylic acid, nicotinic acid, isonicotinic acid, 2-furoic acid, 1-pyrrolecarboxylic acid, monoethyl malonate and ethyl hydrogenphthalate.

Examples of the acid chlorides include salts such as chlorides of the above monobasic acids.

Examples of products from them include neopentyl glycol/caprylic acid capric acid mixed ester, trimethylolpropane/valeric acid heptanoic acid mixed ester, trimethylolpropane/decanoic acid octanoic acid mixed ester, trimethylolpropane nonanoate, and pentaerythritol/haptanoic acid capric acid mixed ester.

The polyol ester (A-1) is preferably a polyol ester having 3 or less hydroxyl groups, and is more preferably a complete ester having no hydroxyl group at a molecular end.

The kinematic viscosity of the polyol ester (A-1) is preferably not more than 3000 cSt at −30° C., and is more preferably not more than 1500 cSt at −30° C.

Paraffin-Based Hydrocarbon Oil (A-2)

The paraffin-based hydrocarbon oil (A-2) is composed of an α-olefin polymer of 25 or more carbon atoms, preferably 30 to 50 carbon atoms. Here, the number of carbon atoms of the paraffin-based hydrocarbon oil (A-2) can be determined by measuring a number-average molecular weight by gel permeation chromatography (GPC) and calculating the number from the measured value.

The α-olefin polymer of 25 or more carbon atoms is a polymer or copolymer of one or more kinds selected from ethylene and α-olefins of 3 to 18 carbon atoms, and is a polymer or copolymer having 25 or more carbon atoms. Specific examples thereof include a trimer of 1-decene, a trimer of 1-undecene, a trimer of 1-dodecene, a trimer of 1-tridecene, a trimer of 1-tetradecene and a copolymer of 1-hexene and 1-pentene.

The kinematic viscosity of the paraffin-based hydrocarbon oil (A-2) is preferably not more than 3000 cSt at −30° C., and is more preferably not more than 1500 cSt at −30° C.

Examples of such paraffin-based hydrocarbon oils (A-2) include products manufactured by Chevron Phillips Chemical Company, Exxon Mobil Chemical Company, Ineos Oligomers, Chemtura Corporation and Idemitsu Kosan Co., Ltd.

Ether Oil (A-3)

The ether oil (A-3) is preferably an ether oil represented by the following general formula (a-3). Since such an ether oil has no hydroxyl group at a molecular end, it is excellent in moisture absorption resistance.

R^a31—(—O—R^a33—)_n—R^a32 (a-3)

In the formula (a-3), R^a31and R^a32are each independently an alkyl group of 1 to 18 carbon atoms or a monovalent aromatic hydrocarbon group of 6 to 18 carbon atoms.

Examples of the alkyl groups of 1 to 18 carbon atoms include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, t-butyl group, n-pentyl group, isopentyl group, t-pentyl group, neopentyl group, n-hexyl group, isohexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group and octadecyl group.

Examples of the monovalent aromatic hydrocarbon groups of 6 to 18 carbon atoms include phenyl group, tolyl group, xylyl group, benzyl group, phenethyl group, 1-phenylethyl group and 1-methyl-1-phenylethyl group.

R^a33is an alkylene group of 1 to 18 carbon atoms or a divalent aromatic hydrocarbon group of 6 to 18 carbon atoms.

Examples of the alkylene groups of 1 to 18 carbon atoms include methylene group, ethylene group, propylene group and butylene group.

Examples of the divalent aromatic hydrocarbon groups of 6 to 18 carbon atoms include phenylene group and 1,2-naphthylene group.

n is an integer of 1 to 5.

As the base oils (A1) for use in the present invention, the polyol esters (A-1) may be used singly or may be used in combination of two or more kinds. The same shall apply to the paraffin-based hydrocarbon oils (A-2) having 25 or more carbon atoms and to the ether oils (A-3). Further, one or more kinds of the polyol esters (A-1) and one or more kinds of the paraffin-based hydrocarbon oils (A-2) having 25 or more carbon atoms may be used in combination. The same shall apply to the paraffin-based hydrocarbon oils (A-2) having 25 or more carbon atoms and the ether oils (A-3), and to the polyol esters (A-1) and the ether oils (A-3). Furthermore, one or more kinds of the polyol esters (A-1), one or more kinds of the paraffin-based hydrocarbon oils (A-2) having 25 or more carbon atoms and one or more kinds of the ether oils (A-3) may be used in combination.

In the case where high stability is required for the lubricating oil composition, such as a case where a plastic member is used in the vicinity of a sliding part, the paraffin-based hydrocarbon oil (A-2) having 25 or more carbon atoms is preferably used. The compatibility is increasing in order of the paraffin-based hydrocarbon oil (A-2), the ether oil (A-3) and the polyol ester (A-1), and therefore, depending upon the components for use in the lubricating oil composition, solubility of those components and low-temperature operating properties of the lubricating oil composition may be controlled by appropriately mixing these base oils.

custom character Solid Lubricant (A2)

The solid lubricant (A2) is a substance capable of reducing sliding resistance when it is in a solid state. The solid lubricant (A2) is, for example, powdery, and therefore, even when a lubricating oil composition containing the solid lubricant (A2) is placed in a low-temperature environment (e.g., −30° C.), the composition is prevented from being solidified and has given fluidity.

Accordingly, not only at ordinary temperature but also at low temperatures, the lubricating oil composition containing the base oil (A1) and the solid lubricant (A2) can be applied to uses to which conventional grease has been applied. In particular, the above lubricating oil composition can be preferably applied to sliding parts (e.g., mainspring in barrel) in a timepiece.

Examples of the solid lubricants (A2) include transition metal sulfides, such as molybdenum disulfide and tungsten disulfide; organomolybdenum compounds; fluororesins, such as polytetrafluoroethylene (PTFE), tetrafluoroethylene/perfluoroalkyl vinyl ether copolymer (PFA), tetrafluoroethylene/hexafluoropropylene copolymer (FEP), tetrafluoroethylene/ethylene copolymer (ETFE), polyvinylidene fluoride (PVDF) and polychlorotrifluoroethylene (PCTFE); and inorganic solid lubricants, such as graphite, hexagonal boron nitride, synthetic mica and talc.

Of these, preferable are fluororesins, transition metal sulfides and graphite, more preferable are PTFE, molybdenum disulfide and graphite, and particularly preferable is PTFE from the viewpoint of a balance between color tone and lubrication properties.

The mean particle diameter of the solid lubricant (A2) is preferably not more than 5 μm, more preferably 0.1 to 5 μm. A mean particle diameter of the above range is preferable from the viewpoints of dispersibility, non-precipitation properties and lubrication properties of the solid lubricant (A2). The mean particle diameter can be measured by, for example, a laser diffraction type particle size distribution measuring device.

The antiwear agent (B) used in the present invention is at least one selected from a neutral phosphate ester (B-1) and a neutral phosphite ester (B-2). The neutral phosphate ester (B-1) is represented by the following general formula (b-1), and the neutral phosphite ester (B-2) is represented by the following general formula (b-2).

Among sliding parts of a mechanical timepiece, there is a sliding part to which a high pressure of not less than 3800 N/mm²is applied, and if a conventional lubricating oil composition is used for this sliding part, a deposit such as worn powder or rust is formed, and the color of the sliding part sometimes changes to dark brown. The reason is thought to be that the conventional lubricating oil composition is manufactured suitably to a quartz type timepiece having low pressure resistance. Further, it is thought that such a phenomenon is also attributable to the fact that the material of the mechanical timepiece is an iron-based material differently from the quartz type timepiece whose material is phosphor bronze or the like.

On the other hand, the lubricating oil composition for a timepiece according to the present invention uses a specific antiwear agent (B), and therefore, the wear resistance and extreme pressure properties of the lubricating oil composition for a timepiece can be improved. That is to say, even when a timepiece is operated using the lubricating oil composition in a sliding part to which great pressure is applied during sliding, formation of a deposit such as worn powder or rust is suppressed, and color change of the sliding part hardly occurs. Thus, according to the lubricating oil composition, even a timepiece having a sliding part to which high pressure is applied can be favorably lubricated.

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In the formula (b-1), R^b11to R^b14each independently represent an aliphatic hydrocarbon group of 10 to 16 carbon atoms.

The aliphatic hydrocarbon group of 10 to 16 carbon atoms may be a straight-chain, branched or cyclic aliphatic hydrocarbon group, and may be a saturated or unsaturated aliphatic hydrocarbon group. Specific examples of the aliphatic hydrocarbon groups of 10 to 16 carbon atoms preferably used include straight-chain alkyl groups, such as decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group and hexadecyl group (cetyl group).

R^b15to R^b18each independently represent a straight-chain or branched alkyl group of 1 to 6 carbon atoms.

Examples of the straight-chain or branched alkyl groups of 1 to 6 carbon atoms include methyl group, ethyl group, n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, isopropyl group, sec-butyl group, isobutyl group, t-butyl group, isopentyl group, t-pentyl group, neopentyl group and isohexyl group.

The neutral phosphate ester (B-1) has specific substituents at R^b15to R^b18, and therefore, even when the lubricating oil composition is used in a sliding part to which great pressure is applied during sliding, wear resistance and extreme pressure properties can be improved. The reason is thought to be that if the neutral phosphate ester has specific substituents at R^b15to R^b18, a film of the lubricating oil composition applied to the sliding part is strengthened.

Particularly when R^b15and R^b17are each a straight-chain alkyl group of 1 to 6 carbon atoms, preferably 1 to 3 carbon atoms, and R^b16and R^b18are each a branched alkyl group of 3 to 6 carbon atoms, preferably 3 to 4 carbon atoms, the effect to improve the aforesaid wear resistance and extreme pressure properties is further enhanced.

R^b191and R^b192each independently represent a hydrogen atom or a straight-chain or branched alkyl group of 1 to 5 carbon atoms.

Examples of the straight-chain or branched alkyl groups of 1 to 5 carbon atoms include methyl group, ethyl group, n-propyl group, n-butyl group, n-pentyl group, isopropyl group, sec-butyl group, isobutyl group, t-butyl group, isopentyl group, t-pentyl group and neopentyl group.

However, the total number of carbon atoms of R^b191and R^b192is 1 to 5. Therefore, when R^b191is, for example, a hydrogen atom, R^b192is a straight-chain or branched alkyl group of 1 to 5 carbon atoms, when R^b191is, for example, a methyl group, R^b192is a straight-chain or branched alkyl group of 1 to 4 carbon atoms, and when R^b191is, for example, an ethyl group, R^b192is a straight-chain or branched alkyl group of 2 to 3 carbon atoms.

It is more preferable that R^b191is a hydrogen atom and R^b192is a straight-chain or branched alkyl group of 1 to 5 carbon atoms, particularly because a film of the lubricating oil composition is further strengthened.

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In the formula (b-2), R^b21to R^b24each independently represent an aliphatic hydrocarbon group of 10 to 16 carbon atoms.

R^b25to R^b28each independently represent a straight-chain or branched alkyl group of 1 to 6 carbon atoms.

The neutral phosphite ester (B-2) has specific substituents at R^b25to R^b28, and therefore, even when the lubricating oil composition is used in a sliding part to which great pressure is applied during sliding, wear resistance and extreme pressure properties can be improved. The reason is thought to be that if the neutral phosphite ester has specific substituents at R^b25to R^b28, a film of the lubricating oil composition applied to the sliding part is strengthened.

Particularly when R^b25and R^b27are each a straight-chain alkyl group of 1 to 6 carbon atoms, preferably 1 to 3 carbon atoms, and R^b26and R^b28are each a branched alkyl group of 3 to 6 carbon atoms, preferably 3 to 4 carbon atoms, the effect to improve the aforesaid wear resistance and extreme pressure properties is further enhanced.

R^b291and R^b292each independently represent a hydrogen atom or a straight-chain or branched alkyl group of 1 to 5 carbon atoms.

However, the total number of carbon atoms of R^b291and R^b292is 1 to 5. Therefore, when R^b291is, for example, a hydrogen atom, R^b292is a straight-chain or branched alkyl group of 1 to 5 carbon atoms, when R^b291is, for example, a methyl group, R^b292is a straight-chain or branched alkyl group of 1 to 4 carbon atoms, and when R^b291is, for example, an ethyl group, R^b292is a straight-chain or branched alkyl group of 2 to 3 carbon atoms.

It is more preferable that R^b291is a hydrogen atom and R^b292is a straight-chain or branched alkyl group of 1 to 5 carbon atoms, particularly because a film of the lubricating oil composition is further strengthened.

It is thought that the neutral phosphite ester (B-2) has higher structural stability when it is used in the lubricating oil composition, and therefore, the neutral phosphite ester (B-2) is still more preferably used.

As the antiwear agents (B) for use in the present invention, the neutral phosphate esters (B-1) may be used singly or may be used in combination of two or more kinds. The same shall apply to the neutral phosphite esters (B-2). Further, one or more kinds of the neutral phosphate esters (B-1) and one or more kinds of the neutral phosphite esters (B-2) may be used in combination.

The antiwear agent (B) is contained in an amount of 0.1 to 15 parts by mass, preferably 0.1 to 8 parts by mass, based on 100 parts by mass of the lubricant component (A). From the viewpoint of enhancement in wear resistance and extreme pressure properties, the antiwear agent is preferably contained in the above proportion.

The lubricating oil composition for a timepiece according to the present invention may further contain another antiwear agent (B′).

Examples of such other antiwear agents (B′) include:

neutral phosphate esters such as tricresyl phosphate, trixylenyl phosphate, trioctyl phosphate, trimethylolpropane phosphate, triphenyl phosphate, tris(nonylphenyl) phosphate, triethyl phosphate, tris(tridecyl) phosphate, tetraphenyl dipropylene glycol diphosphate, tetraphenyl tetra(tridecyl)pentaerythritol tetraphosphate, tetra(tridecyl)-4,4′-isopropylidene diphenyl phosphate, bis(tridecyl)pentaerythritol diphosphate, bis(nonylphenyl)pentaerythritol diphosphate, tristearyl phosphate, distearyl pentaerythritol diphosphate, tris(2,4-di-t-butylphenyl) phosphate, and a hydrogenated bisphenol A/pentaerythritol phosphate polymer; and

neutral phosphite esters such as trioleyl phosphite, trioctyl phosphite, trimethylolpropane phosphite, triphenyl phosphite, tris(nonylphenyl) phosphite, triethyl phosphite, tris(tridecyl) phosphite, tetraphenyl dipropylene glycol diphosphite, tetraphenyl tetra(tridecyl)pentaerythritol tetraphosphite, tetra(tridecyl)-4,4′-isopropylidene diphenyl phosphite, bis(tridecyl)pentaerythritol diphosphite, bis(nonylphenyl)pentaerythritol diphosphite, tristearyl phosphite, distearyl pentaerythritol diphosphite, tris(2,4-di-t-butylphenyl) phosphite and a hydrogenated bisphenol A/pentaerythritol phosphite polymer.

Such other antiwear agents (B′) may be used singly or may be used in combination of two or more kinds.

Such another antiwear agent (B′) is preferably contained in an amount of 0.1 to 8 parts by mass based on 100 parts by mass of the lubricant component (A).

Examples of the antioxidant (C) for use in the present invention include phenol-based antioxidants and amine-based antioxidants. The lubricating oil composition for a timepiece according to the present invention hardly changes in quality for a long period because it contains the antioxidant (C).

Examples of the phenol-based antioxidants include 2,6-di-t-butyl-p-cresol, 2,4,6-tri-t-butylphenol and 4,4′-mehylenebis(2,6-di-t-butylphenol).

Examples of the amine-based antioxidants include a diphenylamine derivative, i.e., a compound in which a hydrogen atom of the benzene ring of diphenylamine is substituted by a straight-chain or branched alkyl group of 1 to 10 carbon atoms because change in quality of the lubricating oil composition is able to be further suppressed. Specific examples of such compounds preferably used include a diphenylamine derivative (C-1) represented by the following general formula (c-1).

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In the formula (c-1), R^c11and R^c12each independently represent a straight-chain or branched alkyl group of 1 to 10 carbon atoms.

Examples of the straight-chain or branched alkyl groups of 1 to 10 carbon atoms include methyl group, ethyl group, n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, isopropyl group, sec-butyl group, isobutyl group, t-butyl group, isopentyl group, t-pentyl group, neopentyl group, isohexyl group, 2-ethylhexyl group, 2,4,4-trimethylpentyl group, and 1,1,3,3-tetramethylbutyl group.

p and q each independently represent an integer of 0 to 5, preferably an integer of 0 to 3. However, p and q do not represent 0 at the same time.

The diphenylamine derivative is obtained by a reaction of, for example, diphenylamine with a compound for introducing a straight-chain or branched alkyl group of 1 to 10 carbon atoms as a substituent (compound having a double bond, such as ethylene, propylene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene, 1-nonene, 1-decene, 2-butene, 2-methylpropene, 3-methyl-1-butene, 2-methyl-1-butene, 4-methyl-1-pentene, 2-ethyl-1-hexene or 2,4,4-trimethylpentene).

Such antioxidants (C) for use in the present invention may be used singly or may be used in combination of two or more kinds.

In particular, as the amine-based antioxidants, one or two or more kinds of the diphenylamine derivatives (C-1) and one or two or more kinds of hindered amine compounds (C-2) represented by the following general formula (c-2) are preferably used in combination.

When the diphenylamine derivative (C-1) and the hindered amine compound (C-2) are combined, even in the case of using the lubricating oil composition in a sliding part to which great pressure is applied during sliding, formation of a deposit such as worn powder or rust is suppressed, color change of the sliding part hardly occurs, and durability can be improved. The reason is thought to be that an antioxidant generally has a function to make harmless an active species produced in the lubricating oil composition during sliding, and when the diphenylamine derivative (C-1) and the hindered amine compound (C-2) are combined, even an active species produced in a sliding part to which great pressure is applied during sliding can be made harmless over a long period of time.

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In the formula (c-2), R^c21and R^c22each independently represent an aliphatic hydrocarbon group of 1 to 10 carbon atoms.

The aliphatic hydrocarbon group of 1 to 10 carbon atoms may be a straight-chain, branched or cyclic aliphatic hydrocarbon group, and may be a saturated or unsaturated aliphatic hydrocarbon group.

Specific examples of the aliphatic hydrocarbon groups of 1 to 10 carbon atoms preferably used include straight-chain or branched alkyl groups, such as methyl group, ethyl group, n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, heptyl group, octyl group, nonyl group, decyl group, isopropyl group, sec-butyl group, isobutyl group, t-butyl group, isopentyl group, t-pentyl group, neopentyl group, isohexyl group and 2-ethylhexyl group. Of these, straight-chain or branched alkyl groups of 5 to 10 carbon atoms are more preferable from the viewpoint of enhancement in durability.

R^c23represents a divalent aliphatic hydrocarbon group of 1 to 10 carbon atoms.

Examples of the divalent aliphatic hydrocarbon groups of 1 to 10 carbon atoms preferably used include divalent straight-chain or branched alkylene groups, such as methylene group, 1,2-ethylene group, 1,3-propylene group, 1,4-butylene group, 1,5-pentylene group, 1,6-hexylene group, 1,7-heptylene group, 1,8-octylene group, 1,9-nonylene group, 1,10-decylene group and 3-methyl-1,5-pentylene group. Of these, divalent straight-chain or branched alkylene groups of 5 to 10 carbon atoms are more preferable from the viewpoint of enhancement in durability.

Particularly from the viewpoint of enhancement in durability at high temperatures, more preferable among the above groups are groups in which the total number of carbon atoms of R^c21, R^c22and R^c23is 16 to 30.

The antioxidant (C) is contained in an amount of 0.01 to 3 parts by mass based on 100 parts by mass of the lubricant component (A). When the diphenylamine derivative (C-1) and the hindered amine compound (C-2) are used in combination, it is preferable that they are each contained in an amount of 0.01 to 1.5 parts by mass based on 100 parts by mass of the lubricant component (A). They are preferably contained in the above proportions from the viewpoint of enhancement in durability.

The lubricating oil composition for a timepiece according to the present invention may further contain a viscosity index improver (D). When the lubricating oil composition contains the viscosity index improver (D), the composition can operate a timepiece more normally.

As the viscosity index improver (D), a hitherto publicly known one can be used, and examples thereof include polyacrylates, polymethacrylates, polyalkylstyrenes, polyesters, isobutylene fumarate, styrene maleate ester, vinyl acetate fumarate ester, α-olefin copolymers, a polybutadiene/styrene copolymer, a polymethyl methacrylate/vinylpyrrolidone copolymer, an ethylene/alkyl acrylate copolymer, polyisobutylene, lithium stearate, or derivatives of lithium stearate.

As the polyacrylates and the polymethacrylates, polymerization products of acrylic acid or methacrylic acid and polymers of C₁-C₁₀-alkyl esters thereof can be used. Of these, polymethacrylate obtained by polymerizing methyl methacrylate is preferable.

Specific examples of the polyalkylstyrenes include polymers of monoalkylstyrenes having substituents of 1 to 18 carbon atoms, such as poly-α-methylstyrene, poly-β-methylstyrene, poly-α-ethylstyrene and poly-β-ethylstyrene.

Examples of the polyesters include polyesters obtained from polyhydric alcohols of 1 to 10 carbon atoms, such as ethylene glycol, propylene glycol, neopentyl glycol and dipentaerythritol, and polybasic acids, such as oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, fumaric acid and phthalic acid.

Specific examples of the α-olefin copolymers include an ethylene/propylene copolymer composed of constitutional repeating units derived from ethylene and constitutional repeating units derived from isopropylene, and reaction products similarly obtained by copolymerizing α-olefins of 2 to 18 carbon atoms, such as ethylene, propylene, butylene and butadiene.

The polyisobutylene preferably has a number-average molecular weight (Mn), as measured by GPC, of 3000 to 80000, and more preferably has Mn of 3000 to 50000 from the viewpoint of lubrication properties.

Specific examples of the derivatives of lithium stearate include lithium stearate in which a hydrogen atom is substituted by a hydroxy group, such as lithium 12-hydroxystearate.

The viscosity index improvers (D) may be used singly or may be used in combination of two or more kinds.

Of these, polyisobutylene, lithium stearate, or a derivative of lithium stearate is more preferably used because more favorable lubrication is enabled even if a timepiece is operated using them in a sliding part to which great pressure is applied during sliding. The reason is thought to be that inclusion of polyisobutylene, lithium stearate, or the derivative of lithium stearate causes an environment in which the antiwear agent (B) more easily functions.

The viscosity index improver (D) is preferably contained in an amount of 0.1 to 8 parts by mass based on 100 parts by mass of the lubricant component (A). From the viewpoint of enhancement in lubrication properties, the viscosity index improver is preferably contained in the above proportion.

The lubricating oil composition for a timepiece according to the present invention may further contain a metal deactivator (E). When the lubricating oil composition contains the metal deactivator (E), the composition can further suppress corrosion of a metal.

From the viewpoint of suppression of corrosion of a metal, the metal deactivator (E) is preferably benzotriazole or its derivative.

Specific examples of the benzotriazole derivatives include 2-(2′-hydroxy-5′-methylphenyl)benzotriazole, 2-[2′-hydroxy-3′,5′-bis(α,α-dimethylbenzyl)phenyl]-benzotriazole, 2-(2′-hydroxy-3′,5′-di-t-butyl-phenyl)-benzotriazole, and compounds having a structure represented by the following formula wherein R, R′ and R″ are each an alkyl group of 1 to 18 carbon atoms, such as 1-(N,N-bis(2-ethylhexyl)aminomethyl)benzotriazole.

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The metal deactivators (E) may be used singly or may be used in combination of two or more kinds.

The metal deactivator (E) is preferably contained in an amount of 0.01 to 3 parts by mass based on 100 parts by mass of the lubricant component (A). From the viewpoint of corrosion prevention, the metal deactivator is preferably contained in the above proportion.

[Timepiece]

In the timepiece according to the present invention, the aforesaid lubricating oil composition for a timepiece has been applied to sliding parts, such as a wheel train part and a mainspring encased in a barrel. The timepiece of the present invention is preferably a timepiece having a sliding part to which great pressure is applied during sliding. Examples of such sliding parts include sliding parts of a mechanical timepiece and sliding parts of an electronic timepiece designed so as to have, for example, many motors. Even if the timepiece of the present invention has a sliding part to which great pressure is applied, formation of a deposit such as worn powder or rust is suppressed during operating and color change of the sliding part hardly occurs because the aforesaid lubricating oil composition for a timepiece has been applied, and therefore, the timepiece of the present invention can stably work over a long period of time.

From the above, the present invention relates to the following.

[1] A lubricating oil composition for a timepiece, comprising a lubricant component (A) containing at least one base oil (A1) selected from a polyol ester (A-1), a paraffin-based hydrocarbon oil (A-2) having 25 or more carbon atoms and an ether oil (A-3), at least one antiwear agent (B) selected from a neutral phosphate ester (B-1) and a neutral phosphite ester (B-2), and an antioxidant (C), wherein

the total acid number of the composition is not more than 0.8 mgKOH/g,

the antiwear agent (B) is contained in an amount of 0.1 to 15 parts by mass based on 100 parts by mass of the lubricant component (A), and the antioxidant (C) is contained in an amount of 0.01 to 3 parts by mass based on 100 parts by mass of the lubricant component (A), and

the neutral phosphate ester (B-1) is represented by the following general formula (b-1) and the neutral phosphite ester (B-2) is represented by the following general formula (b-2).

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Even when a timepiece is operated using the lubricating oil composition for a timepiece in a sliding part to which great pressure is applied, formation of a deposit such as worn powder or rust can be suppressed, and change in color of the sliding part hardly occurs. That is to say, according to the lubricating oil composition, even a mechanical timepiece or the like in which high pressure is applied to its sliding part can be favorably lubricated.

[2] The lubricating oil composition for a timepiece as stated in [1], wherein the polyol ester (A-1) is a polyol ester having no hydroxyl group at a molecular end.

[3] The lubricating oil composition for a timepiece as stated in [1] or [2], wherein the ether oil (A-3) is represented by the following general formula (a-3):

R^a31—(—O—R^a33—)_n—R^a32 (a-3)

wherein R^a31and R^a32are each independently an alkyl group of 1 to 18 carbon atoms or a monovalent aromatic hydrocarbon group of 6 to 18 carbon atoms, R^a33is an alkylene group of 1 to 18 carbon atoms or a divalent aromatic hydrocarbon group of 6 to 18 carbon atoms, and n is an integer of 1 to 5.

[4] The lubricating oil composition for a timepiece as stated in any one of [1] to [3], wherein the antioxidant (C) is an amine-based antioxidant.

Change in quality of the lubricating oil composition can be further suppressed by using the amine-based antioxidant.

[5] The lubricating oil composition for a timepiece as stated in [4], wherein a diphenylamine derivative (C-1) represented by the following general formula (c-1) and a hindered amine compound (C-2) represented by the following general formula (c-2) are contained as the amine-based antioxidants.

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wherein R^c11and R^c12each independently represent a straight-chain or branched alkyl group of 1 to 10 carbon atoms, and p and q each independently represent an integer of 0 to 5 with the proviso that p and q do not represent 0 at the same time,

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wherein R^c21and R^c22each independently represent an aliphatic hydrocarbon group of 1 to 10 carbon atoms, and R^c23represents a divalent aliphatic hydrocarbon group of 1 to 10 carbon atoms.

[6] The lubricating oil composition for a timepiece as stated in any one of [1] to [5], wherein not less than 30% by mass of the lubricant component (A) is the base oil (A1).

[7] The lubricating oil composition for a timepiece as stated in [6], wherein the lubricant component (A) consists of the base oil (A1).

[8] The lubricating oil composition for a timepiece as stated in [6], wherein the lubricant component (A) comprises the base oil (A1) and a solid lubricant (A2).

[9] The lubricating oil composition for a timepiece as stated in [8], wherein the content of the base oil (a1) is 30 to 70% by mass and the content of the solid lubricant (a2) is 70 to 30% by mass, based on 100% by mass of the lubricant component (A).

[10] The lubricating oil composition for a timepiece as stated in any one of [1] to [9], further comprising a viscosity index improver (D).

When the lubricating oil composition comprises the viscosity index improver (D), the composition can operate a timepiece more normally.

[11] The lubricating oil composition for a timepiece as stated in [10], wherein the viscosity index improver (D) is lithium stearate or a derivative of lithium stearate.

[12] The lubricating oil composition for a timepiece as stated in [10], wherein the viscosity index improver (D) is polyisobutylene.

When the lubricating oil composition comprises polyisobutylene, lithium stearate, or a derivative of lithium stearate, more favorable lubrication is enabled even if a timepiece is operated using it in a sliding part to which great pressure is applied during sliding.

[13] The lubricating oil composition for a timepiece as stated in any one of [1] to [12], further comprising a metal deactivator (E).

When the lubricating oil composition comprises the metal deactivator (E), it can further suppress corrosion of a metal.

[14] The lubricating oil composition for a timepiece as stated in [13], wherein the metal deactivator (E) is benzotriazole or a derivative thereof.

When benzotriazole or a derivative thereof is used, corrosion of a metal is further suppressed.

[15] A timepiece to sliding parts of which the lubricating oil composition for a timepiece as stated in any one of [1] to [14] has been applied.

Even when the timepiece has a sliding part to which great pressure is applied during sliding, formation of a deposit such as worn powder or rust is suppressed during operating and color change of the sliding part hardly occurs because the aforesaid lubricating oil composition for a timepiece has been applied, and therefore, the timepiece can stably work over a long period of time.

EXAMPLES

The present invention will be more specifically described hereinafter with reference to the following examples, but it should be construed that the present invention is in no way limited to those examples. In the following description, the term “part(s)” means “part(s) by mass” unless otherwise noted.

In the following specific examples, a base oil (A1) was used as the lubricant component (A).

Example 1-1-1

As the paraffin-based hydrocarbon oil (A-2) of the base oil (A1), a trimer of 1-decene was used, and to 100 parts of this base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as a neutral phosphate ester (B-1) of the antiwear agent (B) and 0.5 part of a diphenylamine derivative (reaction product of diphenylamine with 2,4,4-trimethylpentene (reaction product: IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.)) as the antioxidant (C), to prepare a lubricating oil composition for a timepiece.

The kinematic viscosity of the above base oil at −30° C. was less than 2000 cSt, and the number of carbon atoms thereof was 30.

Example 1-1-2

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-1-1, except that the amount of the neutral phosphate ester (B-1) was changed to 0.1 part.

Example 1-1-3

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-1-1, except that the amount of the neutral phosphate ester (B-1) was changed to 8 parts.

Example 1-1-4

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-1-1, except that the amount of the antioxidant (C) was changed to 0.01 part.

Example 1-1-5

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-1-1, except that the amount of the antioxidant (C) was changed to 3 parts.

Examples 1-2-1 to 1-2-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Example 1-1-1, except that the compounds of Table 1 were each used as the neutral phosphate ester (B-1) instead of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) (R^b11to R^b14=tridecyl group, R^b15, R^b17methyl group, R^b16, R^b18=t-butyl group, R^b191=hydrogen atom, R^b192=n-propyl group).

TABLE 1

Neutral phosphate esters (B-1) used in Examples 1-2-1 to 1-2-6

Example
R^b11-R^b14
R^b15, R^b17
R^b16, R^b18
R^b191
R^b192

1-2-1
decyl
methyl
t-butyl
hydrogen
n-propyl

group
group
group
atom
group

1-2-2
hexadecyl
methyl
t-butyl
hydrogen
n-propyl

group
group
group
atom
group

1-2-3
tridecyl
n-propyl
t-butyl
hydrogen
n-propyl

group
group
group
atom
group

1-2-4
tridecyl
methyl
isopropyl
hydrogen
n-propyl

group
group
group
atom
group

1-2-5
tridecyl
methyl
t-butyl
hydrogen
n-pentyl

group
group
group
atom
group

1-2-6
tridecyl
methyl
t-butyl
ethyl
n-propyl

group
group
group
group
group

Example 1-3-1

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-1-1, except that 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) and 0.5 part of bis(2,2,6,6-tetramethyl-1-(octyloxy)piperidin-4-yl) decanedioate were used as the antioxidant (C) instead of 0.5 part of the diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.).

Example 1-3-2

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-3-1, except that each of the amounts of the diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) and bis(2,2,6,6-tetramethyl-1-(octyloxy)piperidin-4-yl) decanedioate was changed to 0.01 part.

Example 1-3-3

Examples 1-4-1 to 1-4-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Example 1-3-1, except that the compounds of Table 2 were each used instead of bis(2,2,6,6-tetramethyl-1-(octyloxy)piperidin-4-yl) decanedioate (R^c21, R^c22=n-octyl group, R^c23=1,8-octylene group).

TABLE 2

Hindered amine compounds (C-2) used in Examples 1-4-1 to 1-4-6

Example
R^c21
R^c22
R^c23

1-4-1
methyl
methyl
methylene

group
group
group

1-4-2
n-propyl
n-propyl
1,3-propylene

group
group
group

1-4-3
n-pentyl
n-pentyl
1,5-pentylene

group
group
group

1-4-4
n-pentyl
n-pentyl
1,6-hexylene

group
group
group

1-4-5
n-hexyl
n-hexyl
1,6-hexylene

group
group
group

1-4-6
n-decyl
n-decyl
1,10-decylene

group
group
group

Examples 1-5-1 to 1-5-4

Lubricating oil compositions for timepieces were prepared in the same manner as in Example 1-3-1, except that the compounds of Table 3 were each used instead of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.).

TABLE 3

Diphenylamine derivatives (C-1) used in Examples 1-5-1 to 1-5-4

Example
R^c11
R^c12
p
q

1-5-1
ethyl
ethyl
1
1

group
group

1-5-2
n-hexyl
n-hexyl
1
1

group
group

1-5-3
n-decyl
n-decyl
1
1

group
group

1-5-4
t-butyl
t-butyl
1
1

group
group

Example 1-6-1

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-1-1, except that 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphite) was used as the neutral phosphite ester (B-2) instead of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as the neutral phosphate ester (B-1) of the antiwear agent (B).

Example 1-6-2

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-6-1, except that the amount of the neutral phosphite ester (B-2) was changed to 0.1 part.

Example 1-6-3

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-6-1, except that the amount of the neutral phosphite ester (B-2) was changed to 8 parts.

Example 1-6-4

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-6-1, except that the amount of the antioxidant (C) was changed to 0.01 part.

Example 1-6-5

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-6-1, except that the amount of the antioxidant (C) was changed to 3 parts.

Examples 1-7-1 to 1-7-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Example 1-6-1, except that the compounds of Table 4 were each used as the neutral phosphite ester (B-2) instead of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphite) (R^b21to R^b24=tridecyl group, R^b25, R^b27=methyl group, R^b26, R^b28=t-butyl group, R^b291=hydrogen atom, R^b292=n-propyl group).

TABLE 4

Neutral phosphite esters (B-2) used in Examples 1-7-1 to 1-7-6

Example
R^b21-R^b24
R^b25, R²⁷
R^b26, R^b28
R^b291
R^b292

1-7-1
decyl
methyl
t-butyl
hydrogen
n-propyl

group
group
group
atom
group

1-7-2
hexadecyl
methyl
t-butyl
hydrogen
n-propyl

group
group
group
atom
group

1-7-3
tridecyl
n-propyl
t-butyl
hydrogen
n-propyl

group
group
group
atom
group

1-7-4
tridecyl
methyl
isopropyl
hydrogen
n-propyl

group
group
group
atom
group

1-7-5
tridecyl
methyl
t-butyl
hydrogen
n-pentyl

group
group
group
atom
group

1-7-6
tridecyl
methyl
t-butyl
ethyl
n-propyl

group
group
group
group
group

Example 1-8-1

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-6-1, except that 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) and 0.5 part of bis(2,2,6,6-tetramethyl-1-(octyloxy)piperidin-4-yl) decanedioate were used as the antioxidant (C) instead of 0.5 part of the diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.).

Example 1-8-2

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-8-1, except that each of the amounts of the diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) and bis(2,2,6,6-tetramethyl-1-(octyloxy)piperidin-4-yl) decanedioate was changed to 0.01 part.

Example 1-8-3

Examples 1-9-1 to 1-9-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Example 1-8-1, except that the compounds of Table 5 were each used instead of bis(2,2,6,6-tetramethyl-1-(octyloxy)piperidin-4-yl) decanedioate (R^c21, R^c22=n-octyl group, R^c23=1,8-octylene group).

TABLE 5

Hindered amine compounds (C-2) used in Examples 1-9-1 to 1-9-6

Example
R^c21
R^c22
R^c23

1-9-1
methyl
methyl
methylene

group
group
group

1-9-2
n-propyl
n-propyl
1,3-propylene

group
group
group

1-9-3
n-pentyl
n-pentyl
1,5-pentylene

group
group
group

1-9-4
n-pentyl
n-pentyl
1,6-hexylene

group
group
group

1-9-5
n-hexyl
n-hexyl
1,6-hexylene

group
group
group

1-9-6
n-decyl
n-decyl
1,10-decylene

group
group
group

Examples 1-10-1 to 1-10-4

Lubricating oil compositions for timepieces were prepared in the same manner as in Example 1-8-1, except that the compounds of Table 6 were each used instead of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.).

TABLE 6

Diphenylamine derivatives (C-1)

used in Examples 1-10-1 to 1-10-4

Example
R^c11
R^c12
p
q

1-10-1
ethyl
ethyl
1
1

group
group

1-10-2
n-hexyl
n-hexyl
1
1

group
group

1-10-3
n-decyl
n-decyl
1
1

group
group

1-10-4
t-butyl
t-butyl
1
1

group
group

Example 1-11

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 1-1-1.

Specifically, first, 12-hydroxystearic acid and a trimer of 1-decene were put in a container, and heated. In the container, an aqueous LiOH solution was put, the resultant was dehydrated while being continuously warmed to be allowed to react, and was further warmed, and a trimer of 1-decene was input. A trimer of 1-decene was added to adjust a consistency to 200 with a three-roll mill, and a mixture of a derivative of lithium stearate with a trimer of 1-decene was obtained.

Then, 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as the neutral phosphate ester (B-1) and a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C) were added to the mixture, to prepare a lubricating oil composition for a timepiece. Each component was adjusted and added so that the lubricating oil composition contains 5 parts of the neutral phosphate ester (B-1), 0.5 part of the antioxidant (C), and 5 parts of the above lithium 12-hydroxystearate as the viscosity index improver (D), based on 100 parts of the paraffin-based hydrocarbon oil (A-2).

The kinematic viscosity of the above base oil at −30° C. was less than 2000 cSt, and the number of carbon atoms thereof was 30.

Example 1-12

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 1-1-1.

Specifically, as the paraffin-based hydrocarbon oil (A-2) of the base oil (A1), a trimer of 1-decene was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as the neutral phosphate ester (B-1) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 5 parts of polyisobutylene as the viscosity index improver (D), to prepare a lubricating oil composition for a timepiece.

The kinematic viscosity of the above base oil at −30° C. was less than 2000 cSt, and the number of carbon atoms thereof was 30. The number-average molecular weight of polyisobutylene, as measured by GPC, was 3700.

Example 1-13

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 1-6-1.

Then, 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphite) as the neutral phosphite ester (B-2) and a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C) were added to the mixture, to prepare a lubricating oil composition for a timepiece. Each component was adjusted and added so that the lubricating oil composition contains 5 parts of the neutral phosphite ester (B-2), 0.5 part of the antioxidant (C), and 5 parts of the above lithium 12-hydroxystearate as the viscosity index improver (D), based on 100 parts of the paraffin-based hydrocarbon oil (A-2).

The kinematic viscosity of the above base oil at −30° C. was less than 2000 cSt, and the number of carbon atoms thereof was 30.

Example 1-14

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 1-6-1.

Specifically, as the paraffin-based hydrocarbon oil (A-2) of the base oil (A1), a trimer of 1-decene was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphite) as the neutral phosphite ester (B-2) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 5 parts of polyisobutylene as the viscosity index improver (D), to prepare a lubricating oil composition for a timepiece.

Example 1-15

A lubricating oil composition for a timepiece was prepared by further using the metal deactivator (E) in the lubricating oil composition for a timepiece of Example 1-1-1.

Specifically, as the paraffin-based hydrocarbon oil (A-2) of the base oil (A1), a trimer of 1-decene was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as the neutral phosphate ester (B-1) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 0.05 part of benzotriazole as the metal deactivator (E), to prepare a lubricating oil composition for a timepiece.

The kinematic viscosity of the above base oil at −30° C. was less than 2000 cSt, and the number of carbon atoms thereof was 30.

Example 1-16

A lubricating oil composition for a timepiece was prepared by further using the metal deactivator (E) in the lubricating oil composition for a timepiece of Example 1-6-1.

Specifically, as the paraffin-based hydrocarbon oil (A-2) of the base oil (A1), a trimer of 1-decene was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphite) as the neutral phosphite ester (B-2) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 0.05 part of benzotriazole as the metal deactivator (E), to prepare a lubricating oil composition for a timepiece.

The kinematic viscosity of the above base oil at −30° C. was less than 2000 cSt, and the number of carbon atoms thereof was 30.

Examples 2-1-1 to 2-1-5

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-1-1 to 1-1-5, respectively, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 2-2-1 to 2-2-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-2-1 to 1-2-6, respectively, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 2-3-1 to 2-3-3

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-3-1 to 1-3-3, respectively, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 2-4-1 to 2-4-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-4-1 to 1-4-6, respectively, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 2-5-1 to 2-5-4

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-5-1 to 1-5-4, respectively, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 2-6-1 to 2-6-5

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-6-1 to 1-6-5, respectively, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 2-7-1 to 2-7-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-7-1 to 1-7-6, respectively, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 2-8-1 to 2-8-3

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-8-1 to 1-8-3, respectively, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 2-9-1 to 2-9-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-9-1 to 1-9-6, respectively, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 2-10-1 to 2-10-4

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-10-1 to 1-10-4, respectively, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Example 2-11

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 2-1-1.

Specifically, first, 12-hydroxystearic acid and a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) were put in a container, and heated. In the container, an aqueous LiOH solution was put, the resultant was dehydrated while being continuously warmed to be allowed to react, and was further warmed, and a neopentyl glycol/caprylic acid capric acid mixed ester was input. A neopentyl glycol/caprylic acid capric acid mixed ester was added to adjust a consistency to 200 with a three-roll mill, and a mixture of a derivative of lithium stearate with a neopentyl glycol/caprylic acid capric acid mixed ester was obtained.

Example 2-12

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 2-1-1.

Specifically, as the polyol ester (A-1) of the base oil (A1), a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as the neutral phosphate ester (B-1) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 5 parts of polyisobutylene as the viscosity index improver (D), to prepare a lubricating oil composition for a timepiece.

The number-average molecular weight of polyisobutylene, as measured by GPC, was 3700.

Example 2-13

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 2-6-1.

Example 2-14

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 2-6-1.

Specifically, as the polyol ester (A-1) of the base oil (A1), a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphite) as the neutral phosphite ester (B-2) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 5 parts of polyisobutylene as the viscosity index improver (D), to prepare a lubricating oil composition for a timepiece.

The number-average molecular weight of polyisobutylene, as measured by GPC, was 3700.

Example 2-15

A lubricating oil composition for a timepiece was prepared by further using the metal deactivator (E) in the lubricating oil composition for a timepiece of Example 2-1-1.

Specifically, as the polyol ester (A-1) of the base oil (A1), a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as the neutral phosphate ester (B-1) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 0.05 part of benzotriazole as the metal deactivator (E), to prepare a lubricating oil composition for a timepiece.

Example 2-16

A lubricating oil composition for a timepiece was prepared by further using the metal deactivator (E) in the lubricating oil composition for a timepiece of Example 2-6-1.

Specifically, as the polyol ester (A-1) of the base oil (A1), a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphite) as the neutral phosphite ester (B-2) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 0.05 part of benzotriazole as the metal deactivator (E), to prepare a lubricating oil composition for a timepiece.

Examples 3-1-1 to 3-1-5

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-1-1 to 1-1-5, respectively, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 3-2-1 to 3-2-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-2-1 to 1-2-6, respectively, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 3-3-1 to 3-3-3

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-3-1 to 1-3-3, respectively, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 3-4-1 to 3-4-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-4-1 to 1-4-6, respectively, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 3-5-1 to 3-5-4

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-5-1 to 1-5-4, respectively, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 3-6-1 to 3-6-5

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-6-1 to 1-6-5, respectively, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 3-7-1 to 3-7-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-7-1 to 1-7-6, respectively, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 3-8-1 to 3-8-3

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-8-1 to 1-8-3, respectively, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 3-9-1 to 3-9-6

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-9-1 to 1-9-6, respectively, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Examples 3-10-1 to 3-10-4

Lubricating oil compositions for timepieces were prepared in the same manner as in Examples 1-10-1 to 1-10-4, respectively, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Example 3-11

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 3-1-1.

Specifically, first, 12-hydroxystearic acid and an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) were put in a container, and heated. In the container, an aqueous LiOH solution was put, the resultant was dehydrated while being continuously warmed to be allowed to react, and was further warmed, and an alkyl-substituted diphenyl ether was input. An alkyl-substituted diphenyl ether was added to adjust a consistency to 200 with a three-roll mill, and a mixture of a derivative of lithium stearate with an alkyl-substituted diphenyl ether was obtained.

Example 3-12

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 3-1-1.

Specifically, as the ether oil (A-3) of the base oil (A1), an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as the neutral phosphate ester (B-1) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 5 parts of polyisobutylene as the viscosity index improver (D), to prepare a lubricating oil composition for a timepiece.

The number-average molecular weight of polyisobutylene, as measured by GPC, was 3700.

Example 3-13

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 3-6-1.

Example 3-14

A lubricating oil composition for a timepiece was prepared by further using the viscosity index improver (D) in the lubricating oil composition for a timepiece of Example 3-6-1.

Specifically, as the ether oil (A-3) of the base oil (A1), an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphite) as the neutral phosphite ester (B-2) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 5 parts of polyisobutylene as the viscosity index improver (D), to prepare a lubricating oil composition for a timepiece.

The number-average molecular weight of polyisobutylene, as measured by GPC, was 3700.

Example 3-15

A lubricating oil composition for a timepiece was prepared by further using the metal deactivator (E) in the lubricating oil composition for a timepiece of Example 3-1-1.

Specifically, as the ether oil (A-3) of the base oil (A1), an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as the neutral phosphate ester (B-1) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 0.05 part of benzotriazole as the metal deactivator (E), to prepare a lubricating oil composition for a timepiece.

Example 3-16

A lubricating oil composition for a timepiece was prepared by further using the metal deactivator (E) in the lubricating oil composition for a timepiece of Example 3-6-1.

Specifically, as the ether oil (A-3) of the base oil (A1), an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used, and to 100 parts of the base oil were added 5 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphite) as the neutral phosphite ester (B-2) of the antiwear agent (B), 0.5 part of a diphenylamine derivative (IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.) as the antioxidant (C), and 0.05 part of benzotriazole as the metal deactivator (E), to prepare a lubricating oil composition for a timepiece.

Comparative Example 1-1

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-1-1, except that tricresyl phosphate was used instead of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as the antiwear agent.

Comparative Example 1-2

A lubricating oil composition for a timepiece was prepared in the same manner as in Example 1-6-1, except that trioleyl phosphite was used instead of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphite) as the antiwear agent.

Comparative Example 2-1

A lubricating oil composition for a timepiece was prepared in the same manner as in Comparative Example 1-1, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Comparative Example 2-2

A lubricating oil composition for a timepiece was prepared in the same manner as in Comparative Example 1-2, except that a neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C.=less than 2000 cSt) was used as the polyol ester (A-1) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Comparative Example 3-1

A lubricating oil composition for a timepiece was prepared in the same manner as in Comparative Example 1-1, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

Comparative Example 3-2

A lubricating oil composition for a timepiece was prepared in the same manner as in Comparative Example 1-2, except that an alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.) was used as the ether oil (A-3) instead of a trimer of 1-decene that was the paraffin-based hydrocarbon oil (A-2) of the base oil (A1).

[Four-Ball Test]

A four-ball test was conducted according to ASTM-D2783, and wear track diameters were measured with varying loads. Loads in cases in which marked wear started were also determined.

[Timepiece Operating Test (1)]

With regard to Citizen Watch Movement™ (No. 9015) that was a mechanical timepiece, the above-prepared lubricating oil composition for a timepiece was applied to the wheel train part (made of Fe-based alloy) that was a sliding part. This timepiece was continuously operated for 1000 hours under the conditions of −30° C., −10° C., ordinary temperature (25° C.), 80° C., and a humidity of 95% at 45° C. Before and after the test, the sliding part was observed. Specifically, the portions of the sliding part, to which pressures of 8700 N/m², 7960 N/m²and 7465 N/m²had been applied, respectively, were observed. Under any of the above conditions, the test was carried out using 20 samples.

The observation results were evaluated by the criteria described later.

[Timepiece Operating Test (2)]

With regard to Citizen Watch Movement™ (No. 9015) that was a mechanical timepiece, the above-prepared lubricating oil composition for a timepiece was applied to the wheel train part (made of Fe-based alloy) that was a sliding part. This timepiece was subjected to a durability test of 20 years' hands-turning at a rate that was 64 times the normal rate and at ordinary temperature. Before and after the test, the sliding part was observed. Specifically, the portions of the sliding part, to which pressures of 8700 N/m², 7960 N/m²and 7465 N/m²had been applied, respectively, were observed. The test was carried out using 20 samples.

The observation results were evaluated by the criteria described later.

[Timepiece Operating Test (3)]

With regard to Citizen Watch Movement™ (No. 9015) that was a mechanical timepiece, the above-prepared lubricating oil composition for a timepiece was applied to the wheel train part (made of Cu-based alloy) that was a sliding part. This timepiece was continuously operated for 1000 hours at ordinary temperature. Before and after the operation, the sliding part was observed. Specifically, the portions of the sliding part, to which pressures of 8700 N/m², 7960 N/m²and 7465 N/m²had been applied, respectively, were observed. The test was carried out using 20 samples.

The observation results were evaluated by the criteria described later.

[Criteria of Evaluation]

4A: At all of the portions to which pressures of 8700 N/m², 7960 N/m²and 7465 N/m²had been applied, neither color change nor signs of being worn were observed after the test.

3A: At the portion to which a pressure of 8700 N/m²had been applied, signs of being worn were observed though color change was not observed. At the portions to which pressures of 7960 N/m²and 7465 N/m²had been applied, neither color change nor signs of being worn were observed after the test.

2A: At the portions to which pressures of 8700 N/m²and 7960 N/m²had been applied, signs of being worn were observed though color change was not observed. At the portion to which a pressure of 7465 N/m²had been applied, neither color change nor signs of being worn were observed after the test.

A: At the portion to which a pressure of 8700 N/m²had been applied, the color changed to light brown, the surface was worn, and worn powder was observed. At the portion to which a pressure of 7960 N/m²had been applied, signs of being worn were observed though color change was not observed. At the portion to which a pressure of 7465 N/m²had been applied, neither color change nor signs of being worn were observed after the test.

B: At the portion to which a pressure of 8700 N/m²had been applied, the color changed to dark brown, the surface was conspicuously worn, and a large quantity of worn powder was observed. At the portion to which a pressure of 7960 N/m²had been applied, the color changed to light brown, the surface was worn, and worn powder was observed. At the portion to which a pressure of 7465 N/m²had been applied, signs of being worn were observed though color change was not observed.

C: At all of the portions to which pressures of 8700 N/m², 7960 N/m²and 7465 N/m²had been applied, the color changed to dark brown, the surface was conspicuously worn, and a large quantity of worn powder was observed.

[Results of Four-Ball Test]

With regard to the lubricating oil compositions prepared in Example 1-6-1 and Comparative Example 1-2, the evaluation results of the four-ball test are set forth in Table 7 below.

TABLE 7

Load (N) in case in
Wear track

which marked wear started
diameter (mm)

Example 1-6-1
785
4.95

Comparative
618
5.39

Example 1-2

[Results of Timepiece Operating Test]

Evaluation results of the timepiece operating test that was performed on the lubricating oil compositions prepared as previously described are set forth in the following tables.

TABLE 8

Timepiece
Timepiece

operating
operating

Timepiece operating test (1)
test (2)
test (3)

1000 hours
20 years
1000 hours

Wheel train part:
Wheel train
Wheel train

made of Fe-based alloy
part: made of
part: made of

45° C.
Fe-based alloy
Cu-based alloy

Ordinary

Humidity:
Ordinary
Ordinary

Example
−30° C.
−10° C.
temperature
80° C.
95%
temperature
temperature

1-1-1
4A
4A
4A
2A
2A
2A
A

1-1-2
4A
4A
4A
2A
2A
2A
A

1-1-3
4A
4A
4A
2A
2A
2A
A

1-1-4
4A
4A
4A
2A
2A
2A
A

1-1-5
4A
4A
4A
2A
2A
2A
A

1-2-1
4A
4A
4A
2A
2A
2A
A

1-2-2
4A
4A
4A
2A
2A
2A
A

1-2-3
4A
4A
4A
2A
2A
2A
A

1-2-4
4A
4A
4A
2A
2A
2A
A

1-2-5
4A
4A
4A
2A
2A
2A
A

1-2-6
4A
4A
4A
2A
2A
A
A

1-3-1
4A
4A
4A
4A
4A
3A
A

1-3-2
4A
4A
4A
4A
4A
3A
A

1-3-3
4A
4A
4A
4A
4A
3A
A

1-4-1
4A
4A
4A
3A
3A
3A
A

1-4-2
4A
4A
4A
3A
3A
3A
A

1-4-3
4A
4A
4A
3A
3A
3A
A

1-4-4
4A
4A
4A
4A
4A
3A
A

1-4-5
4A
4A
4A
4A
4A
3A
A

1-4-6
4A
4A
4A
4A
4A
3A
A

1-5-1
4A
4A
4A
4A
4A
3A
A

1-5-2
4A
4A
4A
4A
4A
3A
A

1-5-3
4A
4A
4A
4A
4A
3A
A

1-5-4
4A
4A
4A
4A
4A
3A
A

TABLE 9

Timepiece
Timepiece

operating
operating

Timepiece operating test (1)
test (2)
test (3)

1000 hours
20 years
1000 hours

Wheel train part:
Wheel train
Wheel train part:

made of Fe-based alloy
part: made of
made of Cu-based

45° C.
Fe-based alloy
alloy

Ordinary

Humidity:
Ordinary
Ordinary

Example
−30° C.
−10° C.
temperature
80° C.
95%
temperature
temperature

1-6-1
4A
4A
4A
2A
2A
3A
A

1-6-2
4A
4A
4A
2A
2A
3A
A

1-6-3
4A
4A
4A
2A
2A
3A
A

1-6-4
4A
4A
4A
2A
2A
3A
A

1-6-5
4A
4A
4A
2A
2A
3A
A

1-7-1
4A
4A
4A
2A
2A
3A
A

1-7-2
4A
4A
4A
2A
2A
3A
A

1-7-3
4A
4A
4A
2A
2A
3A
A

1-7-4
4A
4A
4A
2A
2A
3A
A

1-7-5
4A
4A
4A
2A
2A
3A
A

1-7-6
4A
4A
4A
2A
2A
2A
A

1-8-1
4A
4A
4A
4A
4A
4A
A

1-8-2
4A
4A
4A
4A
4A
4A
A

1-8-3
4A
4A
4A
4A
4A
4A
A

1-9-1
4A
4A
4A
3A
3A
4A
A

1-9-2
4A
4A
4A
3A
3A
4A
A

1-9-3
4A
4A
4A
3A
3A
4A
A

1-9-4
4A
4A
4A
4A
4A
4A
A

1-9-5
4A
4A
4A
4A
4A
4A
A

1-9-6
4A
4A
4A
4A
4A
4A
A

1-10-1
4A
4A
4A
4A
4A
4A
A

1-10-2
4A
4A
4A
4A
4A
4A
A

1-10-3
4A
4A
4A
4A
4A
4A
A

1-10-4
4A
4A
4A
4A
4A
4A
A

TABLE 10

Timepiece
Timepiece

operating
operating

Timepiece operating test (1)
test (2)
test (3)

1000 hours
20 years
1000 hours

Wheel train part:
Wheel train
Wheel train part:

made of Fe-based alloy
part: made of
made of Cu-based

45° C.
Fe-based alloy
alloy

Ordinary

Humidity:
Ordinary
Ordinary

Example
−30° C.
−10° C.
temperature
80° C.
95%
temperature
temperature

1-11
4A
4A
4A
3A
3A
3A
A

1-12
4A
4A
4A
3A
3A
3A
A

1-13
4A
4A
4A
3A
3A
4A
A

1-14
4A
4A
4A
3A
3A
4A
A

1-15
4A
4A
4A
2A
2A
2A
2A

1-16
4A
4A
4A
2A
2A
3A
2A

TABLE 11

Timepiece
Timepiece

operating
operating

Timepiece operating test (1)
test (2)
test (3)

1000 hours
20 years
1000 hours

Wheel train part:
Wheel train
Wheel train part:

made of Fe-based alloy
part: made of
made of Cu-based

45° C.
Fe-based alloy
alloy

Ordinary

Humidity:
Ordinary
Ordinary

Example
−30° C.
−10° C.
temperature
80° C.
95%
temperature
temperature

2-1-1
4A
4A
4A
2A
2A
2A
A

2-1-2
4A
4A
4A
2A
2A
2A
A

2-1-3
4A
4A
4A
2A
2A
2A
A

2-1-4
4A
4A
4A
2A
2A
2A
A

2-1-5
4A
4A
4A
2A
2A
2A
A

2-2-1
4A
4A
4A
2A
2A
2A
A

2-2-2
4A
4A
4A
2A
2A
2A
A

2-2-3
4A
4A
4A
2A
2A
2A
A

2-2-4
4A
4A
4A
2A
2A
2A
A

2-2-5
4A
4A
4A
2A
2A
2A
A

2-2-6
4A
4A
4A
2A
2A
A
A

2-3-1
4A
4A
4A
4A
4A
3A
A

2-3-2
4A
4A
4A
4A
4A
3A
A

2-3-3
4A
4A
4A
4A
4A
3A
A

2-4-1
4A
4A
4A
3A
3A
3A
A

2-4-2
4A
4A
4A
3A
3A
3A
A

2-4-3
4A
4A
4A
3A
3A
3A
A

2-4-4
4A
4A
4A
4A
4A
3A
A

2-4-5
4A
4A
4A
4A
4A
3A
A

2-4-6
4A
4A
4A
4A
4A
3A
A

2-5-1
4A
4A
4A
4A
4A
3A
A

2-5-2
4A
4A
4A
4A
4A
3A
A

2-5-3
4A
4A
4A
4A
4A
3A
A

2-5-4
4A
4A
4A
4A
4A
3A
A

TABLE 12

Timepiece
Timepiece

operating
operating

Timepiece operating test (1)
test (2)
test (3)

1000 hours
20 years
1000 hours

Wheel train part:
Wheel train
Wheel train part:

made of Fe-based alloy
part: made of
made of Cu-based

45° C.
Fe-based alloy
alloy

Ordinary

Humidity:
Ordinary
Ordinary

Example
−30° C.
−10° C.
temperature
80° C.
95%
temperature
temperature

2-6-1
4A
4A
4A
2A
2A
3A
A

2-6-2
4A
4A
4A
2A
2A
3A
A

2-6-3
4A
4A
4A
2A
2A
3A
A

2-6-4
4A
4A
4A
2A
2A
3A
A

2-6-5
4A
4A
4A
2A
2A
3A
A

2-7-1
4A
4A
4A
2A
2A
3A
A

2-7-2
4A
4A
4A
2A
2A
3A
A

2-7-3
4A
4A
4A
2A
2A
3A
A

2-7-4
4A
4A
4A
2A
2A
3A
A

2-7-5
4A
4A
4A
2A
2A
3A
A

2-7-6
4A
4A
4A
2A
2A
2A
A

2-8-1
4A
4A
4A
4A
4A
4A
A

2-8-2
4A
4A
4A
4A
4A
4A
A

2-8-3
4A
4A
4A
4A
4A
4A
A

2-9-1
4A
4A
4A
3A
3A
4A
A

2-9-2
4A
4A
4A
3A
3A
4A
A

2-9-3
4A
4A
4A
3A
3A
4A
A

2-9-4
4A
4A
4A
4A
4A
4A
A

2-9-5
4A
4A
4A
4A
4A
4A
A

2-9-6
4A
4A
4A
4A
4A
4A
A

2-10-1
4A
4A
4A
4A
4A
4A
A

2-10-2
4A
4A
4A
4A
4A
4A
A

2-10-3
4A
4A
4A
4A
4A
4A
A

2-10-4
4A
4A
4A
4A
4A
4A
A

TABLE 13

Timepiece
Timepiece

operating
operating

Timepiece operating test (1)
test (2)
test (3)

1000 hours
20 years
1000 hours

Wheel train part:
Wheel train
Wheel train part:

made of Fe-based alloy
part: made of
made of Cu-based

45° C.
Fe-based alloy
alloy

Ordinary

Humidity:
Ordinary
Ordinary

Example
−30° C.
−10° C.
temperature
80° C.
95%
temperature
temperature

2-11
4A
4A
4A
3A
3A
3A
A

2-12
4A
4A
4A
3A
3A
3A
A

2-13
4A
4A
4A
3A
3A
4A
A

2-14
4A
4A
4A
3A
3A
4A
A

2-15
4A
4A
4A
2A
2A
2A
2A

2-16
4A
4A
4A
2A
2A
3A
2A

TABLE 14

Timepiece
Timepiece

operating
operating

Timepiece operating test (1)
test (2)
test (3)

1000 hours
20 years
1000 hours

Wheel train part:
Wheel train
Wheel train part:

made of Fe-based alloy
part: made of
made of Cu-based

45° C.
Fe-based alloy
alloy

Ordinary

Humidity:
Ordinary
Ordinary

Example
−30° C.
−10° C.
temperature
80° C.
95%
temperature
temperature

3-1-1
4A
4A
4A
2A
2A
2A
A

3-1-2
4A
4A
4A
2A
2A
2A
A

3-1-3
4A
4A
4A
2A
2A
2A
A

3-1-4
4A
4A
4A
2A
2A
2A
A

3-1-5
4A
4A
4A
2A
2A
2A
A

3-2-1
4A
4A
4A
2A
2A
2A
A

3-2-2
4A
4A
4A
2A
2A
2A
A

3-2-3
4A
4A
4A
2A
2A
2A
A

3-2-4
4A
4A
4A
2A
2A
2A
A

3-2-5
4A
4A
4A
2A
2A
2A
A

3-2-6
4A
4A
4A
2A
2A
A
A

3-3-1
4A
4A
4A
4A
4A
3A
A

3-3-2
4A
4A
4A
4A
4A
3A
A

3-3-3
4A
4A
4A
4A
4A
3A
A

3-4-1
4A
4A
4A
3A
3A
3A
A

3-4-2
4A
4A
4A
3A
3A
3A
A

3-4-3
4A
4A
4A
3A
3A
3A
A

3-4-4
4A
4A
4A
4A
4A
3A
A

3-4-5
4A
4A
4A
4A
4A
3A
A

3-4-6
4A
4A
4A
4A
4A
3A
A

3-5-1
4A
4A
4A
4A
4A
3A
A

3-5-2
4A
4A
4A
4A
4A
3A
A

3-5-3
4A
4A
4A
4A
4A
3A
A

3-5-4
4A
4A
4A
4A
4A
3A
A

TABLE 15

Timepiece
Timepiece

operating
operating

Timepiece operating test (1)
test (2)
test (3)

1000 hours
20 years
1000 hours

Wheel train part:
Wheel train
Wheel train part:

made of Fe-based alloy
part: made of
made of Cu-based

45° C.
Fe-based alloy
alloy

Ordinary

Humidity:
Ordinary
Ordinary

Example
−30° C.
−10° C.
temperature
80° C.
95%
temperature
temperature

3-6-1
4A
4A
4A
2A
2A
3A
A

3-6-2
4A
4A
4A
2A
2A
3A
A

3-6-3
4A
4A
4A
2A
2A
3A
A

3-6-4
4A
4A
4A
2A
2A
3A
A

3-6-5
4A
4A
4A
2A
2A
3A
A

3-7-1
4A
4A
4A
2A
2A
3A
A

3-7-2
4A
4A
4A
2A
2A
3A
A

3-7-3
4A
4A
4A
2A
2A
3A
A

3-7-4
4A
4A
4A
2A
2A
3A
A

3-7-5
4A
4A
4A
2A
2A
3A
A

3-7-6
4A
4A
4A
2A
2A
2A
A

3-8-1
4A
4A
4A
4A
4A
4A
A

3-8-2
4A
4A
4A
4A
4A
4A
A

3-8-3
4A
4A
4A
4A
4A
4A
A

3-9-1
4A
4A
4A
3A
3A
4A
A

3-9-2
4A
4A
4A
3A
3A
4A
A

3-9-3
4A
4A
4A
3A
3A
4A
A

3-9-4
4A
4A
4A
4A
4A
4A
A

3-9-5
4A
4A
4A
4A
4A
4A
A

3-9-6
4A
4A
4A
4A
4A
4A
A

3-10-1
4A
4A
4A
4A
4A
4A
A

3-10-2
4A
4A
4A
4A
4A
4A
A

3-10-3
4A
4A
4A
4A
4A
4A
A

3-10-4
4A
4A
4A
4A
4A
4A
A

TABLE 16

Timepiece
Timepiece

operating
operating

Timepiece operating test (1)
test (2)
test (3)

1000 hours
20 years
1000 hours

Wheel train part:
Wheel train
Wheel train

made of Fe-based alloy
part: made of
part: made of

45° C.
Fe-based alloy
Cu-based alloy

Ordinary

Humidity:
Ordinary
Ordinary

Example
−30° C.
−10° C.
temperature
80° C.
95%
temperature
temperature

3-11
4A
4A
4A
3A
3A
3A
A

3-12
4A
4A
4A
3A
3A
3A
A

3-13
4A
4A
4A
3A
3A
4A
A

3-14
4A
4A
4A
3A
3A
4A
A

3-15
4A
4A
4A
2A
2A
2A
2A

3-16
4A
4A
4A
2A
2A
3A
2A

TABLE 17

Timepiece
Timepiece

operating
operating

Timepiece operating test (1)
test (2)
test (3)

1000 hours
20 years
1000 hours

Wheel train part:
Wheel train
Wheel train

made of Fe-based alloy
part: made of
part: made of

45° C.
Fe-based alloy
Cu-based alloy

Comparative

Ordinary

Humidity:
Ordinary
Ordinary

Example
−30° C.
−10° C.
temperature
80° C.
95%
temperature
temperature

1-1
C
C
C
C
C
C
C

1-2
C
C
C
C
C
C
C

2-1
C
C
C
C
C
C
C

2-2
C
C
C
C
C
C
C

3-1
C
C
C
C
C
C
C

3-2
C
C
C
C
C
C
C

The total acid numbers of the lubricating oil compositions prepared in the above examples and comparative examples were each not more than 0.2 mgKOH/g. With regard to the results of evaluation of the above examples and comparative examples, a difference among the samples was not observed.

Also in the cases where the antioxidants (C) used in Examples 1-1-1, 1-6-1, and 1-11 to 1-16 were changed to other antioxidants (C) set forth in the above Table 3, evaluation results similar to those of Examples 1-1-1, 1-6-1, and 1-11 to 1-16 were obtained. Further, also in the cases where the base oil (A-2) used in Examples 1-1-1, 1-6-1, and 1-11 to 1-16 was changed to another base oil (A-2) that was given as an example in the description of the base oil (A-2) of the aforesaid custom character Base oil (A1), evaluation results similar to those of Examples 1-1-1, 1-6-1, and 1-11 to 1-16 were obtained, also in the cases where the base oil (A-1) used in Examples 2-1-1, 2-6-1, and 2-11 to 2-16 was changed to another base oil (A-1) that was given as an example in the description of the base oil (A-1) of the aforesaid custom character Base oil (A1), evaluation results similar to those of Examples 2-1-1, 2-6-1, and 2-11 to 2-16 were obtained, and also in the cases where the base oil (A-3) used in Examples 3-1-1, 3-6-1, and 3-11 to 3-16 was changed to another base oil (A-3) that was given as an example in the description of the base oil (A-3) of the aforesaid custom character Base oil (A1), evaluation results similar to those of Examples 3-1-1, 3-6-1, and 3-11 to 3-16 were obtained.

With regard to Example 1-6-1 and Comparative Example 1-2, appearances of the sliding parts observed after the timepiece operating test (1) (continuous operation for 1000 hours at ordinary temperature, portion to which a pressure of 7465 N/m²was applied during operation) are shown in FIGS. 1 and 2, respectively. In the case of Example 1-6-1, neither color change nor signs of being worn were observed after the test. On the other hand, in the case of Comparative Example 1-2, a deposit such as worn powder or rust was formed in the sliding part, and the color of the sliding part changed to dark brown.

In the following specific examples, the solid lubricant (A2) was used as the lubricant component (A) together with the base oil (A1).

Example 4-1-1

As the lubricant component (A), a lubricant component consisting of 70% by mass of a trimer of 1-decene, said trimer being the paraffin-based hydrocarbon oil (A-2) of the base oil (A1), and 30% by mass of polytetrafluoroethylene (available from Shamrock Technologies, mean particle diameter: not more than 1 μm) was used. To 100 parts of this lubricant component were added 5.4 parts of 4,4′-butylidenebis(3-methyl-6-t-butylphenyl ditridecyl phosphate) as the neutral phosphate ester (B-1) of the antiwear agent (B) and 0.5 part of a diphenylamine derivative (reaction product of diphenylamine with 2,4,4-trimethylpentene (reaction product: IRGANOX L57 (trade name), available from Ciba Specialty Chemicals Inc.)) as the antioxidant (C), to prepare a lubricating oil composition for a timepiece.

The kinematic viscosity of the above base oil at −30° C. was less than 2000 cSt, and the number of carbon atoms thereof was 30. On this account, the lubricating oil composition obtained by adding the components to the base oil had fluidity even at −30° C.

Examples 4-1-2 to 4-1-18, 5-1-1 to 5-1-4, 6-1-1 to 6-1-6, and 7-1-1 to 7-1-7

Lubricating oil compositions for timepieces were prepared in the same manner as in Example 4-1-1, except that the blending constitution of Example 4-1-1 was changed as shown in Table 18 to Table 20.

[Timepiece Operating Test (4)]

With regard to Citizen Watch Movement™ (No. 82) that was a mechanical timepiece, the above-prepared lubricating oil composition for a timepiece or universal machinery grease “Orelube G-1/3” (available from The Orelube Corp. Japan) was applied to the mainspring in the barrel, said mainspring being a sliding part. Each timepiece was continuously operated for 1000 hours under each of the conditions of −30° C. and ordinary temperature (25° C.). The output during the test was measured by the use of a torque measuring instrument. Before and after the test, the sliding part was observed. Under any of the above conditions, the test was carried out using 20 samples.

The observation results were evaluated by the criteria described later.

[Timepiece Operating Test (5)]

With regard to Citizen Watch Movement™ (No. 82) that was a mechanical timepiece, the above-prepared lubricating oil composition for a timepiece was applied to the mainspring in the barrel, said mainspring being a sliding part. This timepiece was subjected to a durability test of 20 years' hands-turning at a rate that was 64 times the normal rate and at ordinary temperature. Before and after the test, the sliding part was observed. The test was carried out using 20 samples.

The observation results were evaluated by the criteria described later.

[Criteria of Evaluation]

In the timepiece operating test (4), a case where the output rose by not less than 30% as compared with the case where the universal machinery grease “Orelube G-1/3” (available from The Orelube Corp. Japan) was used as the lubricant for the mainspring at ordinary temperature (25° C.) was evaluated as “4A”, a case where the output rose by not less than 20% but less than 30% was evaluated as “3A”, a case where the output rose by not less than 10% but less than 20% was evaluated as “2A”, and a case where the output rose by more than 0% but less than 10% was evaluated as “A”. Here, on the basis of a proportion of a loss of generated torque to a force in the winding of the mainspring when the “Orelube G-1/3” was used, a ratio of this loss proportion reduced when the lubricating oil composition of the above example was used was regarded as an output rise ratio.

When the universal machinery grease “Orelube G-1/3” (available from The Orelube Corp. Japan) was used as the lubricant for the mainspring at −30° C. in the timepiece operating test (4), the grease was solidified, and the watch movement could not be operated. A case where the watch movement could be operated in contrast with this when the lubricating oil composition of the above example was used was evaluated as “A”.

In the timepiece operating test (5), a case where neither color change nor signs of being worn were observed after the test at the mainspring part was evaluated as “2A”, a case where color change was not observed but signs of being worn were observed was evaluated as “A”, a case where the color changed to light brown, the surface was worn, and worn powder was observed was evaluated as “B”, and a case where the color changed to dark brown, the surface was conspicuously worn, and a large quantity of worn powder was observed was evaluated as “C”.

[Results of Timepiece Operating Tests (4) and (5)]

With regard to the lubricating oil compositions prepared as described above, blending constitutions and evaluation results of the timepiece operating tests (4) and (5) are set forth in the following tables.

TABLE 18

Example 4-1

Lubricating oil composition
1
2
3
4
5
6
7
8
9

Lubricant
Base oil
A-2-1
70.0
60.0
51.4
45.9
40.5
30.0
70.0
60.0
51.4

component
(A1) (% by
A-1-1

(A)
mass)
A-3-1

Solid
polytetrafluoroethylene
30.0
40.0
48.6
54.1
59.5
70.0

lubricant
molybdenum disulfide

30.0
40.0
48.6

(A2) (% by
graphite powder

mass)

Lubricant

100
100
100
100
100
100
100
100
100

component

(A)

(part(s) by

mass)

Antiwear
Neutral
4,4′-butylidenebis(3-methyl-
5.4
5.4
5.4
5.4
5.4
5.4
5.4
5.4
5.4

agent
phosphate
6-t-butylphenyl

(B)
ester (B-1)
ditridecyl phosphate)

Neutral
4,4′-butylidenebis(3-methyl-

phosphite
6-t-butylphenyl

ester (B-2)
ditridecyl phosphite)

Antioxidant
Diphenylamine
IRGANOX L57
0.5
0.5
0.5
0.5
0.5
0.5
0.5
0.5
0.5

(C)
derivative

(C-1)

Evaluation

Timepiece operating test (4): output rise
3A
3A
4A
4A
4A
2A
2A
3A
4A

ratio (%) of a case of using the lubricating

oil composition of each example to a case

of using universal machinery grease

“Orelube G-1/3” (available from The Orelube

Corp. Japan) at ordinary temperature (25° C.)

Timepiece operating test (4): −30° C.
A
A
A
A
A
A
A
A
A

Timepiece operating test (5): 20 years,
2A
2A
2A
2A
2A
A
A
2A
2A

mainspring part in barrel

Example 4-1

Lubricating oil composition
10
11
12
13
14
15
16
17
18

Lubricant
Base oil
A-2-1
45.9
40.5
30.0
70.0
60.0
51.4
45.9
40.5
30.0

component
(A1) (% by
A-1-1

(A)
mass)
A-3-1

Solid
polytetrafluoroethylene

lubricant
molybdenum disulfide
54.1
59.5
70.0

(A2) (% by
graphite powder

30.0
40.0
48.6
54.1
59.5
70.0

mass)

Lubricant

100
100
100
100
100
100
100
100
100

component

(A)

(part(s) by

mass)

Antiwear
Neutral
4,4′-butylidenebis(3-methyl-
5.4
5.4
5.4
5.4
5.4
5.4
5.4
5.4
5.4

agent
phosphate
6-t-butylphenyl

(B)
ester (B-1)
ditridecyl phosphate)

Neutral
4,4′-butylidenebis(3-methyl-

phosphite
6-t-butylphenyl

ester (B-2)
ditridecyl phosphite)

Antioxidant
Diphenylamine
IRGANOX L57
0.5
0.5
0.5
0.5
0.5
0.5
0.5
0.5
0.5

(C)
derivative

(C-1)

Evaluation

Timepiece operating test (4): output rise
4A
4A
2A
2A
2A
3A
3A
3A
2A

ratio (%) of a case of using the lubricating

oil composition of each example to a case

of using universal machinery grease

“Orelube G-1/3” (available from The Orelube

Corp. Japan) at ordinary temperature (25° C.)

Timepiece operating test (4): −30° C.
A
A
A
A
A
A
A
A
A

Timepiece operating test (5): 20 years,
2A
2A
A
A
A
2A
2A
2A
A

mainspring part in barrel

A-2-1: trimer of 1-decene

A-1-1: neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C. = less than 2000 cSt)

A-3-1: alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.)

polytetrafluoroethylene (mean particle diameter: not more than 1 μm)

molybdenum disulfide (mean particle diameter: 1.4 μm)

graphite powder (mean particle diameter: 4 μm)

TABLE 19

Example 5-1
Example 6-1

Lubricating oil composition
1
2
3
4
1
2
3
4
5
6

Lubricant
Base oil (A1)
A-2-1
51.4
51.4
51.4
51.4

component
(% by mass)
A-1-1

51.4
45.9
40.5

(A)

A-3-1

51.4
45.9
40.5

Solid
polytetrafluoroethylene
48.6
48.6
48.6
48.6
48.6
54.1
59.5
48.6
54.1
59.5

lubricant
molybdenum disulfide

(A2) (% by
graphite powder

mass)

Lubricant

100
100
100
100
100
100
100
100
100
100

component

(A) (part(s)

by mass)

Antiwear
Neutral
4,4′-butylidenebis(3-methyl-6-t-butylphenyl
0.1
8.0
5.4
5.4
5.4
5.4
5.4
5.4
5.4
5.4

agent (B)
phosphate
ditridecyl phosphate)

ester (B-1)

Neutral
4,4′-butylidenebis(3-methyl-6-t-butylphenyl

phosphite
ditridecyl phosphite)

ester (B-2)

Antioxidant
Diphenylamine
IRGANOX L57
0.5
0.5
0.01
3.0
0.5
0.5
0.5
0.5
0.5
0.5

(C)
derivative

(C-1)

Evaluation

Timepiece operating test (4): output rise ratio (%) of a case of using
2A
4A
4A
4A
4A
4A
4A
4A
4A
4A

the lubricating oil composition of each example to a case of using

universal machinery grease “Orelube G-1/3” (available from The Orelube

Corp. Japan) at ordinary temperature (25° C.)

Timepiece operating test (4): −30° C.
A
A
A
A
A
A
A
A
A
A

Timepiece operating test (5): 20 years, mainspring part in barrel
2A
2A
A
2A
2A
2A
2A
2A
2A
2A

A-2-1: trimer of 1-decene

A-1-1: neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C. = less than 2000 cSt)

A-3-1: alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.)

polytetrafluoroethylene (mean particle diameter: not more than 1 μm)

molybdenum disulfide (mean particle diameter: 1.4 μm)

graphite powder (mean particle diameter: 4 μm)

TABLE 20

Example 7-1

Lubricating oil composition
1
2
3
4
5
6
7

Lubricant
Base oil (A1) (% by
A-2-1
51.4
51.4
51.4
51.4
51.4
51.4
51.4

component
mass)
A-1-1

(A)

A-3-1

Solid lubricant (A2)
polytetrafluoroethylene
48.6

48.6
48.6
48.6
48.6

(% by mass)
molybdenum disulfide

48.6

graphite powder

48.6

Lubricant component

100
100
100
100
100
100
100

(A) (part(s) bymass)

Antiwear
Neutral phosphate
4,4′-butylidenebis(3-methyl-6-t-butylphenyl

agent (B)
ester (B-1)
ditridecyl phosphate)

Neutral phosphite
4,4′-butylidenebis(3-methyl-6-t-butylphenyl
5.4
5.4
5.4
0.1
8.0
5.4
5.4

ester (B-2)
ditridecyl phosphite)

Antioxidant
Diphenylamine
IRGANOX L57
0.5
0.5
0.5
0.5
0.5
0.01
3.0

(C)
derivative (C-1)

Evaluation

Timepiece operating test (4): output rise ratio (%) of a case of using the
4A
4A
3A
2A
4A
4A
4A

lubricating oil composition of each example to a case of using universal machinery

grease “Orelube G-1/3” (available from The Orelube Corp. Japan) at ordinary

temperature (25° C.)

Timepiece operating test (4): −30° C.
A
A
A
A
A
A
A

Timepiece operating test (5): 20 years, mainspring part in barrel
2A
2A
2A
2A
2A
A
2A

A-2-1: trimer of 1-decene

A-1-1: neopentyl glycol/caprylic acid capric acid mixed ester (kinematic viscosity at −30° C. = less than 2000 cSt)

A-3-1: alkyl-substituted diphenyl ether (trade name: MORESCO-HILUBE LB32, available from MATSUMURA OIL Co., Ltd.)

polytetrafluoroethylene (mean particle diameter: not more than 1 μm)

molybdenum disulfide (mean particle diameter: 1.4 μm)

graphite powder (mean particle diameter: 4 μm)

The total acid numbers of the lubricating oil compositions prepared in the above examples were each not more than 0.2 mgKOH/g. With regard to the results of evaluation of the above examples, a difference among the samples was not observed.

[Four-Ball Test]

A four-ball test was conducted according to ASTM-D2783, and loads in cases in which marked wear started and in which seizure started were determined.

[Results of Four-Ball Test]

With regard to the lubricating oil composition prepared in Example 4-1-3 and to the universal machinery grease “Orelube G-1/3” (available from The Orelube Corp. Japan), the evaluation results of the four-ball test is set forth in Table 20 below. The consistency (25° C.) of the lubricating oil composition of Example 4-1-3, based on JIS K 2220, was 320, whereas the consistency (25° C.) of “Orelube G-1/3” was 273.

TABLE 21

Load (N) in case in
Load (N) in case in

which marked wear started
which seizure started

Example 4-1-3
981
6080

Orelube G-1/3
490
1961

Number	Name	Date	Kind
3174931	Matson et al.	Mar 1965	A
3239464	Matson et al.	Mar 1966	A
3318811	Conradi	May 1967	A
5186852	Ishida et al.	Feb 1993	A
8741820	Akao	Jun 2014	B2
20030050197	Akao	Mar 2003	A1
20030109387	Akao et al.	Jun 2003	A1
20030162870	Kimura	Aug 2003	A1
20050014658	Akao	Jan 2005	A1
20080220999	Chase et al.	Sep 2008	A1
20110077178	Chase	Mar 2011	A1
20110257053	Akao	Oct 2011	A1
20110306530	Manabe	Dec 2011	A1
20120028861	Douglas	Feb 2012	A1
20150337233	Akao	Nov 2015	A1

Number	Date	Country
1364190	Aug 2002	CN
1462320	Dec 2003	CN
1578826	Feb 2005	CN
1715381	Jan 2006	CN
0387979	Sep 1990	EP
0 612 837	Aug 1994	EP
2003192919	Jul 2003	JP
EP 0612837	Aug 1994	NL
WO 9620263	Jul 1996	WO
0159043	Aug 2001	WO
2008109523	Sep 2008	WO
2014115602	Jul 2014	WO

Lubricating oil composition for timepiece and timepiece

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

Field of Search

CPC

International Classifications

Disclaimer

Term Extension

Abstract

Description

Claims

Priority Claims (1)

PCT Information

US Referenced Citations (15)

Foreign Referenced Citations (12)

Non-Patent Literature Citations (3)

Related Publications (1)

Entry
EIC structure search Jul. 2016.
International Search Report of PCT/JP2014/050454 dated Feb. 18, 2014 [PCT/ISA/210].
Communication dated Jun. 22, 2016 from the European Patent Office in counterpart application No. 14743589.5.